Name | Beckwith-Wiedemann Syndrome |
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Synonyms | Beckwith Wiedemann Syndrome | BWCR, INCLUDED | BWS | EMG Syndrome | EMG Syndromes | Exomphalos-Macroglossia-Gigantism Syndrome | Syndrome, Beckwith-Wiedemann | Syndrome, EMG | Syndromes, EMG | Syndromes, Wiedemann-Beckwith (WBS) | Syndrome, Wiedemann-Beckwith | Syndrome, Wiedemann-Beckwith (WBS) | Wiedemann Beckwith Syndrome | Wiedemann-Beckwith Syndrome | Wiedemann-Beckwith Syndromes (WBS) | Wiedemann Beckwith Syndrome (WBS) | Wiedemann-Beckwith Syndrome (WBS) | WIEDEMANN-BECKWITH SYNDROME;WBS BECKWITH-WIEDEMANN SYNDROME CHROMOSOME REGION, INCLUDED |
Definition | A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities. |
Categories | Congenital abnormality | Genetic disease (inborn) |
MeSH® ID | D001506 |
OMIM® ID | 130650 |
External Links |
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Diseases
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Diseases
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Diseases
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Beckwith-Wiedemann Syndrome
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Franceschini Vardeu Guala syndrome |